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Microtubule assembly in meiotic extract requires glycogen

The assembly of microtubules during mitosis requires many identified components, such as γ-tubulin ring complex (γ-TuRC), components of the Ran pathway (e.g., TPX2, HuRP, and Rae1), and XMAP215/chTOG. However, it is far from clear how these factors function together or whether more factors exist. In...

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Detalles Bibliográficos
Autores principales: Groen, Aaron C., Coughlin, Margaret, Mitchison, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164461/
https://www.ncbi.nlm.nih.gov/pubmed/21737678
http://dx.doi.org/10.1091/mbc.E11-02-0158
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author Groen, Aaron C.
Coughlin, Margaret
Mitchison, Timothy J.
author_facet Groen, Aaron C.
Coughlin, Margaret
Mitchison, Timothy J.
author_sort Groen, Aaron C.
collection PubMed
description The assembly of microtubules during mitosis requires many identified components, such as γ-tubulin ring complex (γ-TuRC), components of the Ran pathway (e.g., TPX2, HuRP, and Rae1), and XMAP215/chTOG. However, it is far from clear how these factors function together or whether more factors exist. In this study, we used biochemistry to attempt to identify active microtubule nucleation protein complexes from Xenopus meiotic egg extracts. Unexpectedly, we found both microtubule assembly and bipolar spindle assembly required glycogen, which acted both as a crowding agent and as metabolic source glucose. By also reconstituting microtubule assembly in clarified extracts, we showed microtubule assembly does not require ribosomes, mitochondria, or membranes. Our clarified extracts will provide a powerful tool for activity-based biochemical fractionations for microtubule assembly.
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spelling pubmed-31644612011-11-16 Microtubule assembly in meiotic extract requires glycogen Groen, Aaron C. Coughlin, Margaret Mitchison, Timothy J. Mol Biol Cell Articles The assembly of microtubules during mitosis requires many identified components, such as γ-tubulin ring complex (γ-TuRC), components of the Ran pathway (e.g., TPX2, HuRP, and Rae1), and XMAP215/chTOG. However, it is far from clear how these factors function together or whether more factors exist. In this study, we used biochemistry to attempt to identify active microtubule nucleation protein complexes from Xenopus meiotic egg extracts. Unexpectedly, we found both microtubule assembly and bipolar spindle assembly required glycogen, which acted both as a crowding agent and as metabolic source glucose. By also reconstituting microtubule assembly in clarified extracts, we showed microtubule assembly does not require ribosomes, mitochondria, or membranes. Our clarified extracts will provide a powerful tool for activity-based biochemical fractionations for microtubule assembly. The American Society for Cell Biology 2011-09-01 /pmc/articles/PMC3164461/ /pubmed/21737678 http://dx.doi.org/10.1091/mbc.E11-02-0158 Text en © 2011 Groen et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Groen, Aaron C.
Coughlin, Margaret
Mitchison, Timothy J.
Microtubule assembly in meiotic extract requires glycogen
title Microtubule assembly in meiotic extract requires glycogen
title_full Microtubule assembly in meiotic extract requires glycogen
title_fullStr Microtubule assembly in meiotic extract requires glycogen
title_full_unstemmed Microtubule assembly in meiotic extract requires glycogen
title_short Microtubule assembly in meiotic extract requires glycogen
title_sort microtubule assembly in meiotic extract requires glycogen
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164461/
https://www.ncbi.nlm.nih.gov/pubmed/21737678
http://dx.doi.org/10.1091/mbc.E11-02-0158
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